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Wnt proteins are lipid-modified and can act as stem cell growth factors
Abstract
Wnt signalling is involved in numerous events in animal development, including the proliferation of stem cells and the specification of the neural crest. Wnt proteins are potentially important reagents in expanding specific cell types, but in contrast to other developmental signalling molecules such as hedgehog proteins and the bone morphogenetic proteins, Wnt proteins have never been isolated in an active form. Although Wnt proteins are secreted from cells, secretion is usually inefficient and previous attempts to characterize Wnt proteins have been hampered by their high degree of insolubility. Here we have isolated active Wnt molecules, including the product of the mouse Wnt3a gene. By mass spectrometry, we found the proteins to be palmitoylated on a conserved cysteine. Enzymatic removal of the palmitate or site-directed and natural mutations of the modified cysteine result in loss of activity, and indicate that the lipid is important for signalling. The purified Wnt3a protein induces self-renewal of haematopoietic stem cells, signifying its potential use in tissue engineering.
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“Studies have revealed that the Wnt proteins are glycosylated in the endoplasmic reticulum and also are palmitolated.9,10”
From Wnt signal transduction pathways (2008) · cites this paper as [10]
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Large-scale analysis of the yeast proteome by multidimensional protein identification technology
Washburn, M. P., Wolters, D. A., & Yates, J. R. (2001) · Nature Biotechnology · doi:10.1038/85686 · Cited by 4,768
Self-citationPhase separation of integral membrane proteins in Triton X-114 solution.
Bordier, C. (1981) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)69848-0 · Cited by 3,324
Polakis, P. (2000) · Genes & Development · doi:10.1101/gad.14.15.1837 · Cited by 3,183
Wnt signaling: a common theme in animal development
Cadigan, K. M., & Nusse, R. (1997) · Genes & Development · doi:10.1101/gad.11.24.3286 · Cited by 2,567
Self-citationA role for Wnt signalling in self-renewal of haematopoietic stem cells
Reya, T., Duncan, A. W., Ailles, L., Domen, J., Scherer, D. C., Willert, K., Hintz, L., Nusse, R., & Weissman, I. L. (2003) · Nature · doi:10.1038/nature01593 · Cited by 2,159
Self-citationThe β-Catenin/TCF-4 Complex Imposes a Crypt Progenitor Phenotype on Colorectal Cancer Cells
van de Wetering, M., Sancho, E., Verweij, C., de Lau, W., Oving, I., Hurlstone, A., van der Horn, K., Batlle, E., Coudreuse, D., Haramis, A.-P., et al. (2002) · Cell · doi:10.1016/s0092-8674(02)01014-0 · Cited by 2,030
Tabb, D. L., McDonald, W. H., & Yates, J. R. (2002) · Journal of Proteome Research · doi:10.1021/pr015504q · Cited by 1,369
Self-citationIdentification of a Palmitic Acid-modified Form of Human Sonic hedgehog
Pepinsky, R. B., Zeng, C., Wen, D., Rayhorn, P., Baker, D. P., Williams, K. P., Bixler, S. A., Ambrose, C. M., Garber, E. A., Miatkowski, K., et al. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.22.14037 · Cited by 754
Wnt Signaling and an APC-Related Gene Specify Endoderm in Early C. elegans Embryos
Rocheleau, C. E., Downs, W. D., Lin, R., Wittmann, C., Bei, Y., Cha, Y.-H., Ali, M., Priess, J. R., & Mello, C. C. (1997) · Cell · doi:10.1016/s0092-8674(00)80531-0 · Cited by 660
Shotgun identification of protein modifications from protein complexes and lens tissue
MacCoss, M. J., McDonald, W. H., Saraf, A., Sadygov, R. G., Clark, J., Tasto, J. J., Gould, K. L., Wolters, D. A., Washburn, M. P., Weiss, A., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.122231399 · Cited by 593
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Liu, X., Li, J., Yu, Z., Li, J., Sun, R., & Kan, Q. (2016) · Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics · doi:10.3727/096504016x14747300207374 · Cited by 61
FGF‐4 regulates neural progenitor cell proliferation and neuronal differentiation
Kosaka, N., Kodama, M., Sasaki, H., Yamamoto, Y., Takeshita, F., Takahama, Y., Sakamoto, H., Kato, T., Terada, M., & Ochiya, T. (2006) · The FASEB Journal · doi:10.1096/fj.05-5293fje · Cited by 62
Murdolo, G., Bartolini, D., Tortoioli, C., Piroddi, M., Iuliano, L., & Galli, F. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.08.007 · Cited by 61
Hung, T., Hsu, S., Cheng, C., Choo, K., Tseng, C., Chen, T., Lan, Y., Huang, T., Lai, H., Chen, C., et al. (2014) · Oncotarget · doi:10.18632/oncotarget.2631 · Cited by 60
A gradient of Shh establishes mutually repressing somitic cell fates induced by Nkx3.2 and Pax3
Cairns, D. M., Sato, M. E., Lee, P. G., Lassar, A. B., & Zeng, L. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.08.024 · Cited by 60
Kumar, D., & Lassar, A. B. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.07.038 · Cited by 60
Cited2 is required for normal hematopoiesis in the murine fetal liver
Chen, Y., Haviernik, P., Bunting, K. D., & Yang, Y. (2007) · Blood · doi:10.1182/blood-2007-01-066316 · Cited by 62
Mohinta, S. (2007) · Frontiers in bioscience · doi:10.2741/2368 · Cited by 61
The microenvironment of the embryonic neural stem cell: Lessons from adult niches?
Lathia, J. D., Rao, M. S., Mattson, M. P., & ffrench‐Constant, C. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21319 · Cited by 61
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Wang, C., Jamal, L., & Janes, K. A. (2011) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.159 · Cited by 65
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Thomas, B. L., Eldridge, S. E., Nosrati, B., Fallas, M. E. A., Thorup, A., Nalesso, G., Caxaria, S., Barawi, A., Nicholson, J. G., Perretti, M., et al. (2021) · Journal of Extracellular Vesicles · doi:10.1002/jev2.12088 · Cited by 59
Palmitoylation of Hedgehog Proteins
Buglino, J. A., & Resh, M. D. (2012) · Vitamins and hormones · doi:10.1016/b978-0-12-394622-5.00010-9 · Cited by 59
The enhanced effect of lupeol on the destruction of gastric cancer cells by NK cells
Wu, X., Liu, J., Lu, X., Chen, F., Zhou, Z.-H., Wang, T., Zhu, S.-P., & Fei, S. (2013) · International Immunopharmacology · doi:10.1016/j.intimp.2013.04.017 · Cited by 59
Sweetser, D. A., Peniket, A. J., Haaland, C. M., Blomberg, A. A., Zhang, Y., Zaidi, S. T., Dayyani, F., Zheng, Z. S., Heerema, N. A., Boultwood, J., et al. (2005) · Genes Chromosomes and Cancer · doi:10.1002/gcc.20236 · Cited by 60
Wang, B.-E., Wang, X.-D., Ernst, J. A., Polakis, P. G., & Gao, W. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002186 · Cited by 60
Carpenter, A. C., Smith, A. N., Wagner, H. E., Cohen‐Tayar, Y., Rao, S., Wallace, V. A., Ashery‐Padan, R., & Lang, R. A. (2015) · Development · doi:10.1242/dev.120022 · Cited by 59
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Ohta, H., Sekulovic, S., Bakovic, S., Eaves, C. J., Pineault, N., Gasparetto, M., Smith, C. A., Sauvageau, G., & Humphries, R. K. (2007) · Experimental Hematology · doi:10.1016/j.exphem.2007.02.012 · Cited by 59
Vas, V., Szilágyi, L. S., Pálóczi, K., & Uher, F. (2004) · Journal of Leukocyte Biology · doi:10.1189/jlb.1003462 · Cited by 59
Cryo-EM structure of human Wntless in complex with Wnt3a
Zhong, Q., Zhao, Y., Ye, F., Xiao, Z., Huang, G., Xu, M. M., Zhang, Y., Zhan, X., Sun, K., Wang, Z., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24731-3 · Cited by 56
Cross-Talk between p53 and Wnt Signaling in Cancer
Xiao, Q., Werner, J., Venkatachalam, N., Boonekamp, K. E., Ebert, M. P. A., & Zhan, T. (2022) · Biomolecules · doi:10.3390/biom12030453 · Cited by 59
Wingless/Wnt signaling in Drosophila: The pattern and the pathway
Bejsovec, A. (2013) · Molecular Reproduction and Development · doi:10.1002/mrd.22228 · Cited by 55
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Feng, Q., & Gao, N. (2014) · Journal of Cellular Physiology · doi:10.1002/jcp.24853 · Cited by 60
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Dhamdhere, G. R., Fang, M. Y., Jiang, J., Katherine, L., Cheng, D., Olveda, R., Liu, B., Mulligan, K. A., Carlson, J. C., Ransom, R. C., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0083650 · Cited by 58
Hasegawa, K., Yasuda, S.-Y., Teo, J.-L., Nguyen, C., McMillan, M., Hsieh, C., Suemori, H., Nakatsuji, N., Yamamoto, M., Miyabayashi, T., et al. (2011) · Stem Cells Translational Medicine · doi:10.5966/sctm.2011-0033 · Cited by 58
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Ching, W., & Nusse, R. (2006) · Cell · doi:10.1016/j.cell.2006.04.018 · Cited by 58
Self-citationWnt signaling: the good and the bad
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Xiong, J., Yu, Q., Zhang, J., & Mably, J. D. (2008) · Circulation Research · doi:10.1161/circresaha.107.163907 · Cited by 58
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Tríbulo, P., Leão, B. C. S., Lehloenya, K. C., Mingoti, G. Z., & Hansen, P. J. (2017) · Biology of Reproduction · doi:10.1093/biolre/iox048 · Cited by 58
Boerboom, D., White, L. D., Dalle, S., Courty, J., & Richards, J. S. (2006) · Cancer Research · doi:10.1158/0008-5472.can-05-3493 · Cited by 60
Satoh, K., Kasai, M., Ishidao, T., Tago, K.-I., Ohwada, S., Hasegawa, Y., Senda, T., Takada, S., Nada, S., Nakamura, T., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401733101 · Cited by 59
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Moore, K. A. (2004) · Current Opinion in Hematology · doi:10.1097/01.moh.0000133652.06863.47 · Cited by 58
Abdelhamed, Z. A., Natarajan, S., Wheway, G., Inglehearn, C. F., Toomes, C., Johnson, C. A., & Jagger, D. J. (2015) · Disease Models & Mechanisms · doi:10.1242/dmm.019083 · Cited by 53
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Ramayo‐Caldas, Y., Ballester, M., Fortes, M. R. S., Esteve‐Codina, A., Castelló, A., Noguera, J. L., Fernández, A. I., Miguel Pérez-enciso, A., Reverter, A., & Folch, J. M. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-232 · Cited by 61
Buglino, J. A., & Resh, M. D. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011195 · Cited by 57
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Liu, W., Shaver, T. M., Balasa, A., Ljungberg, M. C., Wang, X., Wen, S., Nguyen, H., & den Veyver, I. B. V. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032331 · Cited by 57
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Hsieh, T., Hsu, C., Tsai, C., Chiu, C., Liang, S., Wang, T., Kuo, P., Long, C., & Tsai, E. (2016) · Scientific Reports · doi:10.1038/srep19156 · Cited by 57
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Bertrand, J., Kräft, T., Gronau, T., Sherwood, J., Rutsch, F., Lioté, F., Dell’Accio, F., Lohmann, C. H., Bollmann, M., Held, A., et al. (2020) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2019-216648 · Cited by 57
Podsypanina, K., Li, Y., & VARMUS, H. E. (2004) · BMC Medicine · doi:10.1186/1741-7015-2-24 · Cited by 57
Kobune, M., Ito, Y., Kawano, Y., Sasaki, K., Uchida, H., Nakamura, K., Dehari, H., Chiba, H., Takimoto, R., Matsunaga, T., et al. (2004) · Blood · doi:10.1182/blood-2003-09-3347 · Cited by 57
Wexler, E. M., Rosen, E., Lu, D., Osborn, G. E., Martin, E., Raybould, H., & Geschwind, D. H. (2011) · Science Signaling · doi:10.1126/scisignal.2002282 · Cited by 56
Wöhrle, S., Wallmen, B., & Hecht, A. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.00555-07 · Cited by 56
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Ukita, K., Hirahara, S., Oshima, N., Imuta, Y., Yoshimoto, A., Jang, C., Oginuma, M., Saga, Y., Behringer, R. R., Kondoh, H., et al. (2009) · Mechanisms of Development · doi:10.1016/j.mod.2009.08.003 · Cited by 55
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Macé, M., Galiacy, S. D., Erraud, A., Mejía, J. E., Etchevers, H., Allouche, M., Desjardins, L., Calvas, P., & Malecaze, F. (2011) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.10-70981 · Cited by 54
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Metadata
- Authors
- Willert, K., Brown, J. D., Danenberg, E., Duncan, A. W., Weissman, I. L., Reya, T., Yates, J. R., & Nusse, R.
- Affiliations
- Howard Hughes Medical Institute (US)
- Duke University (US)
- Stanford Medicine (US)
- Scripps Research Institute (US)
- ORCID
- Venue
- Nature
- Published
- 2003-04-27
- Volume
- 423
- Issue
- 6938
- Pages
- 448-452
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2147864074
- Cited by
- 2,257
- References
- 30
- Citations by year
- 2026: 40 · 2025: 42 · 2024: 48 · 2023: 54 · 2022: 63 · 2021: 63 · 2020: 78 · 2019: 87 · 2018: 86 · 2017: 90 · 2016: 100 · 2015: 101 · 2014: 99 · 2013: 106 · 2012: 133
- FWCI
- 48.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK067834)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Hedgehog Signaling Pathway Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- Wnt proteins, Wnt3a, palmitoylation, lipid modification, cysteine modification, Wnt signaling, hematopoietic stem cells, stem cell self-renewal, stem cell growth factor, tissue engineering, neural crest specification, protein purification
- MeSH terms
- Amino Acid Sequence, Animals, Cell Differentiation, Cell Division, Cysteine, Cytoskeletal Proteins, Drosophila melanogaster, Growth Substances, Hematopoietic Stem Cells, L Cells, Molecular Sequence Data, Palmitic Acids, Proteins, Solubility, Xenopus laevis, Signal Transduction, Trans-Activators, Mutagenesis, Site-Directed, Conserved Sequence, Hematopoietic Stem Cell Transplantation, Xenopus Proteins, Zebrafish Proteins, Lipid Metabolism, Wnt Proteins, beta Catenin, Mice, Wnt3 Protein, Wnt3A Protein
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